Clinical Trial Manager (PM) - Mexico

Medpace; Ciudad de México; On-site; MXN 800,000 - 1,100,000; Full time

Benefits offered by this job

Equity grants

Competitive compensation program

Office-based with occasional WFH after

Comprehensive health, retirement, and

PTO benefits

Job summary

Medpace is seeking seasoned Clinical Trial Managers / Project Managers to join our Mexico City office, leading day-to-day operations for trials across Phases 1–4. You will coordinate cross-functional teams, ensure adherence to ICH/GCP, and serve as primary sponsor contact for study deliverables.

You will oversee site quality, risk management, and vendor oversight while collaborating with global teams. Fluency in English is required; on-site work in Mexico City is expected.

Qualifications

• Bachelor’s degree in a health-related field required; advanced degree preferred.
• 5+ years as a project/clinical trial manager within a CRO.
• Experience in Phases 1-4; Phases 2-3 preferred. Fluency in English.

Responsibilities

• Manage day-to-day operations of the project per contract and ICH/GCP.
• Serve as primary Sponsor contact for operational issues and study deliverables.
• Maintain knowledge of protocol, therapeutic area, and indications.
• Provide cross-functional oversight of internal project team members and training.
• Review and input for study protocol, edits, data analysis plan, and final report.
• Develop operational project plans and manage risk assessment/execution.
• Oversee study vendor management and site quality.
• Directly supervise Clinical Research Associates and monitoring deliverables.

Skills

Project management

Leadership

Cross-functional coordination

English fluency

Education

Bachelor's degree in health-related field

Advanced degree preferred

Job description

Join Medpace in our Mexico City office! Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Mexico City, Mexico. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

Responsibilities

• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables
• Maintain in depth knowledge of protocol, therapeutic area, and indication
• Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
• Develop operational project plans
• Manage risk assessment and execution
• Responsible for management of study vendor
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Qualifications

• Bachelor’s degree in a health-related field required; Advanced degree in a health-related field preferred
• Experience in Phases 1-4; Phases 2-3 preferred
• 5+ years as a project/clinical trial manager within a CRO
• Management of overall project timeline
• Bid defense experience, preferred
• Strong leadership skills
• Fluency in English

*We kindly ask to send applications in English.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.